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KLFMED Burette Infusion Sets - Indonesia BPOM Medical Device Registration

KLFMED Burette Infusion Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220187. The device is manufactured by WENZHOU KLF MEDICAL PLASTICS CO., LTD.. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDICAL GREY INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : C
KLFMED Burette Infusion Sets
Analysis ID: AKL 20902220187

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDICAL GREY INTERNATIONAL

AR Address

JL. KALIMANTAN NO 22 GKB MANYAR

Registration Date

Mar 02, 2022

Expiry Date

Aug 31, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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